Addison's disease

Addison's disease

Addison's disease


Overview

Addison's disease, also known as adrenal insufficiency, is a rare condition characterized by insufficient production of certain hormones in the body. This disorder occurs when the adrenal glands fail to produce adequate amounts of cortisol and often, insufficient levels of aldosterone.

Addison's disease can affect individuals of any age and poses potential life-threatening complications. Treatment typically involves hormone replacement therapy to address the hormone deficiencies.


Symptoms

The symptoms of Addison's disease typically occurs gradually over months, sometimes leading individuals to overlook them initially. However, symptoms may exacerbate during times of stress, such as illness or injury. Common symptoms include:

  • Profound fatigue
  • Unintentional weight loss and decreased appetite
  • Hyperpigmentation of the skin
  • Low blood pressure, occasionally resulting in fainting
  • Cravings for salt
  • Episodes of low blood sugar (hypoglycemia)
  • Gastrointestinal disturbances like nausea, diarrhea, or vomiting
  • Abdominal discomfort
  • Muscle and joint pain
  • Mood changes, including irritability and Depression
  • Hair loss or sexual dysfunction in some cases
  • Acute adrenal failure, also referred to as addisonian crisis

In some instances, the symptoms of Addison's disease may manifest suddenly, leading to acute adrenal failure, a potentially life-threatening condition requiring immediate medical attention.


Causes

Addison's disease stems from damage to the adrenal glands, situated above the kidneys. These glands play a vital role in hormone production, affecting numerous bodily functions. Damage to the adrenal cortex, responsible for producing cortisol and aldosterone, results in hormone deficiencies. Causes of adrenal gland failure include:

  • Autoimmune diseases targeting the adrenal cortex
  • Infectious diseases like tuberculosis affecting the adrenal glands
  • Metastatic cancer spreading to the adrenal glands
  • Hemorrhage into the adrenal glands
  • Medications interfering with cortisol production or action

Secondary adrenal insufficiency can also occur due to insufficient production of adrenocorticotropic hormone (ACTH) by the pituitary gland, affecting cortisol production indirectly.


Risk Factors

While most cases of Addison's disease occur sporadically, certain factors may increase the risk:

  • History of pituitary or adrenal gland disorders or surgeries
  • Genetic mutations affecting adrenal function, such as congenital adrenal hyperplasia
  • Coexistence with other autoimmune endocrine disorders
  • Traumatic brain injury


Complications

Untreated Addison's disease can lead to severe complications, including:

  • Addisonian crisis, precipitated by physical stressors like injury or infection, characterized by life-threatening symptoms such as low blood pressure and electrolyte imbalances
  • Increased susceptibility to other autoimmune disorders


Prevention

Prevention of Addison's disease is not feasible, but steps can be taken to prevent addisonian crises:

  • Seeking medical advice for persistent fatigue or unexplained weight loss
  • Proper management of Addison's disease during illness or stress, including adjustments in corticosteroid dosage
  • Prompt medical attention during severe illness or inability to take medications

Despite concerns regarding potential side effects of corticosteroid therapy, individuals with Addison's disease are less likely to experience adverse effects due to carefully adjusted replacement therapy. Regular medical follow-up ensures optimal dosage adjustments.